UASt regulatory sequences drive expression of an inverted repeat.
The expression of Plc21CGD11359 under the control of Scer\GAL4elav-C155 induces a significant decrease in larval NMJ mEPSP frequency only in males, and no changes in mEPSP amplitude in both males and females, as compared to controls.
Expression of Plc21CGD11359 driven by Scer\GAL4phm.PO leads to developmental delay/arrest at the larval stage. Prothoracic gland cells of third instar Scer\GAL4phm.PO>Plc21CGD11359 larvae show significant decreases in both macro and micro calcium spikes.
Flies expressing Plc21CGD11359 in LN[[v]] neurons under the control of Scer\GAL4P0.5.Pdf exhibit a longer rhythm period (25.1hr) compared to controls.
Adults expressing Plc21CGD11359 under the control of Scer\GAL4elav.PLu (in the presence of Dcr-2Scer\UAS.cDa to increase the efficiency of RNAi) do not show a significant defect in avoidance of noxious temperature (46[o]C) compared to control flies.
The electroantennograms of animals expressing Plc21CGD11359 under the control of either Scer\GAL4Or83b.2.642.T:Hsim\VP22 or Scer\GAL4Gα49B.PS show a significant decrease in amplitude compared to controls in response to a number of odours (ethyl acetate, butanol, propionic acid, benzaldehyde and iso-amyl acetate).
The response of ab2 large basiconic hairs in the antenna of animals expressing Plc21CGD11359 under the control of Scer\GAL4Or83b.2.642.T:Hsim\VP22 is significantly different from that of control cells; the firing frequency of the mutant ab2a neuron in response to ethyl acetate is strongly reduced compared to controls.
Plc21CGD11359, Scer\GAL4P0.5.Pdf has abnormal circadian rhythm phenotype, non-suppressible by GαoGTP.UAS, Scer\GAL4P0.5.Pdf
Plc21CGD11359, Scer\GAL4elav-C155 is an enhancer | female limited of partially lethal - majority die phenotype of Scer\GAL4elav-C155, cacRQ,SL.UAS.EGFP
Plc21CGD11359, Scer\GAL4elav-C155 is a suppressor of abnormal neurophysiology | larval stage phenotype of Scer\GAL4elav-C155, cacRQ,SL.UAS.EGFP
Plc21CGD11359, Scer\GAL4P0.5.Pdf is a suppressor of abnormal circadian rhythm phenotype of GαoGTP.UAS, Scer\GAL4P0.5.Pdf
Plc21CGD11359, Scer\GAL4elav-C155 is a suppressor of embryonic/larval neuromuscular junction | larval stage phenotype of Scer\GAL4elav-C155, cacRQ,SL.UAS.EGFP
Female larvae expressing cacRQ,SL.UAS.EGFP under the control of Scer\GAL4elav-C155 exhibit a significant increase in NMJ mEPSP amplitude and frequency; the increased amplitude is suppressed by Plc21CGD11359 co-expression.
Expression of Plc21CGD11359 prevents the compensatory increase in quantal content seen in response to reduced quantal size when GluRIICdsRNA.Scer\UAS.cBa is expressed using multiple pre- and post-synaptic drivers (Scer\GAL4elav-C155, Scer\GAL4sca.PC and Scer\GAL4C57). Evoked neurotransmission is therefore disrupted. Muscle expression of Plc21CGD11359 (under the control of Scer\GAL4C57) do not prevent the compensatory increase and evoked neurotransmission is unaffected.
Co-expression of Plc21CGD11359 with G-oα47AGTP.Scer\UAS in LN[[v]] neurons under the control of Scer\GAL4P0.5.Pdf results in strong rhythms. These flies exhibit longer period rhythms (24.7hr) than control flies.
The electroantennograms of animals co-expressing Plc21CGD11359 and Gα49BdsRNA.Scer\UAS.1f1 under the control of Scer\GAL4Or83b.2.642.T:Hsim\VP22 show a significant decrease in amplitude compared to controls in response to a number of odours (ethyl acetate, butanol, propionic acid, benzaldehyde and iso-amyl acetate).